ArticleJACC. Case reports2026
Organizing Hematoma Involving a Native Tricuspid Valve: Fatal Case of Cardiac Behçet Disease-Hughes-Stovin Syndrome Overlap.
Article in JACC. Case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundBehçet disease (BD) is a multisystem vasculitis with variable cardiovascular involvement. Hughes-Stovin syndrome (HSS), featuring pulmonary artery aneurysms and venous thrombosis, is considered a rare variant within the BD spectrum. Intracardiac mass formation in either vasculitis is exceptionally rare. CASE SUMMARY: A 32-year-old man with prior mucocutaneous ulcers presented with hemoptysis and chest pain. Multimodality imaging revealed pulmonary arterial thrombosis and lobulated intracardiac mass attached to the native tricuspid valve (TV). Histopathology showed inflammatory organizing hematoma. Despite anticoagulation and valve replacement, the patient developed pulmonary artery pseudoaneurysms and died from fatal hemorrhage. DISCUSSION: Eight similar cases in the literature revealed a pattern of TV masses, pulmonary artery aneurysms, and hemoptysis in young male patients, suggesting a cardiac-predominant BD-HSS overlap syndrome. TAKE-HOME MESSAGES: An under-recognized syndrome shares overlapping features of BD and HSS, a common denominator being unusual TV masses. In patients with pulmonary artery involvement, immunosuppressive therapy is critical, and anticoagulation requires caution given aneurysmal rupture risk.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.